Canonical Allele Identifier: CA402949656

Gene: STK11

Linked Data

• ClinVar Variation Id: 428776
• ClinVar RCV Id: RCV000492208 ; RCV000557192 ; RCV001548233
• dbSNP Id: rs1131690940
• gnomAD v4: 19-1220641-C-T
• COSMIC: COSM13480 ; COSM4278102
• MyVariant Identifiers: chr19:g.1220640C>T (hg19) ; chr19:g.1220641C>T (hg38)
• PubMed: PMID:9850045 ; PMID:9887330 ; PMID:15188174 ; PMID:16287113 ; PMID:16707622 ; PMID:17026623 ; PMID:23415580 ; PMID:23515270 ; PMID:26607058

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220641C>T , CM000681.2:g.1220641C>T	GRCh38
NC_000019.9:g.1220640C>T , CM000681.1:g.1220640C>T	GRCh37
NC_000019.8:g.1171640C>T	NCBI36
NG_007460.2:g.36235C>T , LRG_319:g.36235C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.658C>T	ENSP00000490268.2:p.Gln220Ter
ENST00000585748.3:c.286C>T	ENSP00000477641.2:p.Gln96Ter
ENST00000585851.2:c.484C>T	ENSP00000467912.2:p.Gln162Ter
ENST00000326873.12:c.658C>T MANE Select	ENSP00000324856.6:p.Gln220Ter
ENST00000652231.1:c.658C>T	ENSP00000498804.1:p.Gln220Ter
ENST00000326873.11:c.658C>T	ENSP00000324856.6:p.Gln220Ter
ENST00000586243.5:c.658C>T	ENSP00000467240.2:p.Gln220Ter
ENST00000586358.5:n.556C>T
ENST00000589152.5:n.748C>T
ENST00000591133.2:n.629C>T
NM_000455.4:c.658C>T , LRG_319t1:c.658C>T	NP_000446.1:p.Gln220Ter
XM_005259617.1:c.658C>T	XP_005259674.1:p.Gln220Ter
XM_005259618.3:c.658C>T	XP_005259675.1:p.Gln220Ter
XM_011528209.1:c.436C>T	XP_011526511.1:p.Gln146Ter
XR_936204.1:n.1283C>T
XM_005259617.3:c.658C>T	XP_005259674.1:p.Gln220Ter
XM_011528209.2:c.436C>T	XP_011526511.1:p.Gln146Ter
XR_001753738.2:n.1283C>T
XR_001753739.1:n.1283C>T
XR_001753740.2:n.1283C>T
NM_000455.5:c.658C>T MANE Select	NP_000446.1:p.Gln220Ter